Evidence map›Paper›PMID 40416903›Full record

ArticleCase reports in hematology2025

Unusual Long-Term Survival in an Adult Patient With Langerhans Cell Histiocytosis and Central Nervous System Involvement: A Case Report.

María José Miranda Pallarés, Tomás Álvaro Naranjo, Anna Vidal Rodriguez, Francisca Martínez Madueño

Abstract readCase Reports
In one paragraph

Article in Case reports in hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

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No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

María José Miranda PallarésMedical Oncology Unit, Institut d'Oncologia de la Catalunya Sud (IOCS), Hospital Universitari Sant Joan de Reus, Reus 43204, Catalonia, Spain.ORCID https://orcid.org/0009-0003-0049-4717
Tomás Álvaro NaranjoService of Pathology, Hospital de Tortosa Verge de la Cinta-ICS Ebre, Tortosa, Tarragona, Spain.ORCID https://orcid.org/0000-0002-7858-2384
Anna Vidal RodriguezMedical Oncology Unit, Institut d'Oncologia de la Catalunya Sud (IOCS), Hospital Universitari Sant Joan de Reus, Reus 43204, Catalonia, Spain.ORCID https://orcid.org/0000-0002-6720-2702
Francisca Martínez MadueñoMedical Oncology Unit, Institut d'Oncologia de la Catalunya Sud (IOCS), Hospital Universitari Sant Joan de Reus, Reus 43204, Catalonia, Spain.ORCID https://orcid.org/0000-0002-0507-1831

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Langerhans cell histiocytosis (LCH) in adults is a rare condition. The disease presents with focal or multifocal involvement of a single organ/system or focal or disseminated multisystem disease. Involvement of the central nervous system (CNS) is also infrequent, with diabetes insipidus as a common manifestation of posterior pituitary lesions. Biopsy-proven diagnosis with the observation of characteristic Langerhans cells infiltrate with positive immunohistochemistry of S100 protein, CD1a, and CD68 cells. The patient presented generalized lymphadenopathy and was diagnosed with low-risk single-system LCH-based distinctive pathological findings in a lymph node biopsy. During the disease, CNS involvement was documented and the patient received different sequential therapeutic schemes, achieving complete remission that has been maintained for 8 years. The prolonged duration of remission with disappearance of lymphadenopathy and CNS lesions in an adult patient with LCH is an unusual clinical observation.

Indexed as

adultBRAF mutationdendritic cellsdiabetes insipidusLangerhans cell histiocytosisLangerhans cellslymphadenopathyMAP2K1 mutations

Identifiers

PMID40416903
PMCPMC12101904

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